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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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Georgirene D. Vladutiu

Department of Pediatrics

School of Medicine & Biomedical Sciences

State University of New York at Buffalo

14209

USA

[email]@*.buffalo.edu

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Department of Pediatrics, School of Medicine & Biomedical Sciences, State University of New York at Buffalo, 14209, USA. 2000 - 2002
  • Departments of Pediatrics, Neurology, and Pathology, School of Medicine and Biomedical Sciences, USA. 2002
  • Associate Professor, Departments of Pediatrics, Neurology, and Pathology, USA. 2000
  • State University of New York at Buffalo, 14209, USA. 1999
  • Robert Guthrie Biochemical Genetics Laboratory, Children's Hospital of Buffalo, USA. 1997

References

  1. Laboratory diagnosis of metabolic myopathies. Vladutiu, G.D. Muscle. Nerve (2002) [Pubmed]
  2. Phenotypic variability among first-degree relatives with carnitine palmitoyltransferase II deficiency. Vladutiu, G.D., Bennett, M.J., Fisher, N.M., Smail, D., Boriack, R., Leddy, J., Pendergast, D.R. Muscle. Nerve (2002) [Pubmed]
  3. Heterozygosity: an expanding role in proteomics. Vladutiu, G.D. Mol. Genet. Metab. (2001) [Pubmed]
  4. The molecular diagnosis of metabolic myopathies. Vladutiu, G.D. Neurol. Clin (2000) [Pubmed]
  5. A variable myopathy associated with heterozygosity for the R503C mutation in the carnitine palmitoyltransferase II gene. Vladutiu, G.D., Bennett, M.J., Smail, D., Wong, L.J., Taggart, R.T., Lindsley, H.B. Mol. Genet. Metab. (2000) [Pubmed]
  6. Rapid, cost-effective gene mutation screening for carnitine palmitoyltransferase II deficiency using whole blood on filter paper. Smail, D., Gambino, L., Boles, C., Vladutiu, G.D. Clin. Chem. (1999) [Pubmed]
  7. Advances in the genetic mechanisms of mitochondrial disease. Vladutiu, G.D. Curr. Opin. Neurol. (1997) [Pubmed]
 
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